(S,R,S)-AHPC-Me-CO-CH2-PEG3-NH2

发表于由

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白，专注于信号通路和疾病研究领域。

(S,R,S)-AHPC-Me-CO-CH2-PEG3-NH2  纯度: 95.06%

(S,R,S)-AHPC-Me-CO-CH2-PEG3-NH2 是一种合成的 E3 连接酶配体结合物，它结合了 VHL 配体和 linker。(S,R,S)-AHPC-Me-CO-CH2-PEG3-NH2 可用于 PROTAC BRD4 Degrader-5 (HY-133737) 和 PROTAC BRD4 Degrader-5-CO-PEG3-N3 (HY-133736)。

(S,R,S)-AHPC-Me-CO-CH2-PEG3-NH2

(S,R,S)-AHPC-Me-CO-CH2-PEG3-NH2 Chemical Structure

CAS No. : 2409538-69-6

规格 价格 是否有货 数量
25 mg ￥5500 In-stock
100 mg ￥12500 In-stock
200 mg   询价  
500 mg   询价  

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生物活性

(S,R,S)-AHPC-Me-CO-CH2-PEG3-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the a VHL ligand and a linker. (S,R,S)-AHPC-Me-CO-CH2-PEG3-NH2 can be used in PROTAC BRD4 Degrader-5 (HY-133737) and PROTAC BRD4 Degrader-5-CO-PEG3-N3 (HY-133736)[1].

IC50 & Target

VHL

 

体外研究
(In Vitro)

PROTAC BRD4 Degrader-5 is a PROTAC-based BRD4 degrader. PROTAC BRD4 Degrader-5 can potent degrade BRD4 in HER2 positive and negative breast cancer cell lines[1].
PROTAC BRD4 Degrader-5-CO-PEG3-N3 is a PROTAC-linker Conjugate for PAC, comprises the BRD4 degrader GNE-987 and PEG-based linker[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

633.80

Formula

C31H47N5O7S
CAS 号

2409538-69-6
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献

  • [1]. Marı A Maneiro, et al. Antibody-PROTAC Conjugates Enable HER2-Dependent Targeted Protein Degradation of BRD4. ACS Chem Biol. 2020 Jun 19;15(6):1306-1312.

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